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FDA 510(k)

MEDCOMP SUBCLAVIAN CATHETER

K-Number: K801672 · 1980-12-18

Decision Date1980-12-18
Product CodeLFJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDCOMP SUBCLAVIAN CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc.. It received FDA 510(k) clearance on 1980-12-18 under 510(k) number K801672. The device is classified under product code LFJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDCOMP SUBCLAVIAN CATHETER?

MEDCOMP SUBCLAVIAN CATHETER is a medical device that received FDA 510(k) clearance on 1980-12-18. The listed applicant is Medical Components, Inc.. The 510(k) number is K801672.

When did MEDCOMP SUBCLAVIAN CATHETER receive FDA 510(k) clearance?

MEDCOMP SUBCLAVIAN CATHETER received FDA 510(k) clearance on 1980-12-18, under 510(k) number K801672.

Who is the listed applicant for MEDCOMP SUBCLAVIAN CATHETER?

The FDA 510(k) record lists Medical Components, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDCOMP SUBCLAVIAN CATHETER?

The FDA product code for MEDCOMP SUBCLAVIAN CATHETER is LFJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Medical Components, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 61 devices →

Related Devices (Code: LFJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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